Disorder overview: Phenylketonuria is a genetic disorder that disrupts the metabolism of the amino acid phenylalanine. It's caused by the deficiency of a liver enzyme called phenylalanine hydroxylase. The normal phenylalanine metabolism is blocked, so if eaten the enzyme accumulates in the blood and tissues. This, if left untreated, can result in irreversible mental retardation, neurological abnormalities, seizures, eczema and behavioral problems. [1]
To help with PKU you need to have a low protein diet and even if you have a low protein diet it is hard to survive because you would be very weak.
To help with PKU you need to have a low protein diet and even if you have a low protein diet it is hard to survive because you would be very weak.
Less than 200,000 cases in the USA
Symptoms:
PKU could cause you to become weak because you can't get amino acids throughout the whole body.
https://www.youtube.com/watch?v=a0urPofZiuY
a video on what pku is
References:
http://web.b.ebscohost.com/src_ic/detail/detail?vid=2&sid=86aa1deb-0abc-4810-bd34-2dc34794be28%40sessionmgr101&bdata=#AN=86194421&db=t6o
https://www.mayoclinic.org/diseases-conditions/phenylketonuria/symptoms-causes/syc-20376302
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=716